Browse by UCL people
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Number of items: 50.
Article
Buchanan, James;
Hill, Melissa;
Vass, Caroline M;
Hammond, Jennifer;
Riedijk, Sam;
Klapwijk, Jasmijn E;
Harding, Eleanor;
... Lewis, Celine; + view all
(2022)
Factor's that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey.
Prenatal Diagnosis
10.1002/pd.6159.
(In press).
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Chitty, LS;
Wright, D;
Hill, M;
Verhoef, TI;
Daley, R;
Lewis, C;
Mason, S;
... Morris, S; + view all
(2016)
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
BMJ
, 354
, Article i3426. 10.1136/bmj.i3426.
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Dore, Rhys;
Nizza, Isabella E;
Mitchison, Hannah M;
Lewis, Celine;
(2024)
‘Don’t let it hold you back’ — The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis.
Journal of Health Psychology
10.1177/13591053231223912.
(In press).
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Friedrich, B;
Vindrola-Padros, C;
Lucassen, AM;
Patch, C;
Clarke, A;
Lakhanpaul, M;
Lewis, C;
(2024)
"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England.
Frontiers in Genetics
, 14
, Article 1282034. 10.3389/fgene.2023.1282034.
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Gurasashvili, Jana;
Silverio, Sergio A;
Hill, Melissa;
Peter, Michelle;
Stafford-Smith, Bethany;
Lewis, Celine;
(2023)
The disequilibrium of hope: A grounded theory analysis of parents' experiences of receiving a "no primary finding" result from genome sequencing.
Journal of Genetic Counseling
10.1002/jgc4.1818.
(In press).
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Hammond, J;
Klapwijk, JE;
Riedijk, S;
Lou, S;
Ormond, KE;
Vogel, I;
Hui, L;
... Lewis, C; + view all
(2022)
Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design.
PLoS ONE
, 17
(1)
, Article e0261898. 10.1371/journal.pone.0261898.
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Hammond, J;
Garner, I;
Hill, M;
Patch, C;
Hunter, A;
Searle, B;
Sanderson, SC;
(2021)
Animation or leaflet: Does it make a difference when educating young people about genome sequencing?
Patient Education and Counseling
10.1016/j.pec.2021.02.048.
(In press).
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Hammond, J;
Klapwijk, JE;
Hill, M;
Lou, S;
Ormond, KE;
Diderich, KEM;
Riedijk, S;
(2020)
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty.
Journal of Genetic Counseling
10.1002/jgc4.1311.
(In press).
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Harding, E;
Hammond, J;
Chitty, LS;
Hill, M;
Lewis, C;
(2020)
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review.
Prenatal Diagnosis
, 40
(8)
pp. 1028-1039.
10.1002/pd.5729.
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Hill, M;
Hammond, J;
Sharmin, M;
Lewis, C;
Heathfield, M;
Crowe, B;
Götherström, C;
... DeVile, C; + view all
(2021)
Living with Osteogenesis Imperfecta: A qualitative study exploring experiences and psychosocial impact from the perspective of patients, parents and professionals.
Disability and Health Journal
, Article 101168. 10.1016/j.dhjo.2021.101168.
(In press).
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Hill, M;
Hammond, J;
Lewis, C;
Mellis, R;
Clement, E;
Chitty, LS;
(2020)
Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges.
European Journal of Human Genetics
10.1038/s41431-020-0667-z.
(In press).
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Hill, M;
Lewis, C;
Chitty, LS;
(2016)
Stakeholder attitudes and needs regarding cell-free fetal DNA testing.
Current Opinion in Obstetrics and Gynecology
, 28
(2)
pp. 125-131.
10.1097/GCO.0000000000000251.
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Hill, M;
Lewis, C;
Riddington, M;
Crowe, B;
DeVile, C;
David, AL;
Semler, O;
... Chitty, LS; + view all
(2019)
Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta.
European Journal of Human Genetics
10.1038/s41431-019-0387-4.
(In press).
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Hill, M;
Lewis, C;
Riddington, M;
Crowe, B;
DeVile, C;
Gotherstrom, C;
Chitty, L;
(2019)
Exploring the impact of Osteogenesis Imperfecta on families: A mixed-methods systematic review.
Disability and Health Journal
, 12
(3)
pp. 340-349.
10.1016/j.dhjo.2018.12.003.
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Hill, M;
Wright, D;
Daley, R;
Lewis, C;
McKay, F;
Mason, S;
Lench, N;
... Chitty, LS; + view all
(2014)
Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol.
BMC Pregnancy Childbirth
, 14
(1)
, Article 229. 10.1186/1471-2393-14-229.
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Hui, L;
Szepe, E;
Halliday, J;
Lewis, C;
(2020)
Maternity health care professionals' views and experiences of fetal genomic uncertainty: A review.
Prenatal Diagnosis
, 40
(6)
pp. 652-660.
10.1002/pd.5673.
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Hunter, A;
Lewis, C;
Hill, M;
Chitty, LS;
Leeson-Beevers, K;
McInnes-Dean, H;
Harvey, K;
... Thomson, K; + view all
(2023)
Public and patient involvement in research to support genome services development in the UK.
Journal of Translational Genetics and Genomics
, 7
pp. 17-26.
10.20517/jtgg.2022.19.
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Hutchinson, C;
Shelmerdine, SC;
Lewis, C;
Parmenter, J;
Simcock, IC;
Ward, L;
Ashworth, MT;
... Sebire, NJ; + view all
(2019)
Minimally invasive perinatal and pediatric autopsy with laparoscopically assisted tissue sampling: feasibility and experience of the MinImAL procedure.
Ultrasound in Obstetrics & Gynecology
, 54
(5)
pp. 661-669.
10.1002/uog.20211.
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Klapwijk, JE;
Srebniak, MI;
Go, ATJI;
Govaerts, LCP;
Lewis, C;
Hammond, J;
Hill, M;
... Riedijk, SR; + view all
(2021)
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies.
Clinical Genetics
10.1111/cge.14010.
(In press).
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Lewis, C;
(2023)
Genomic testing for rare disease diagnosis—where are we now, and where should we be heading? The reflections of a behavioural scientist.
European Journal of Human Genetics
10.1038/s41431-023-01439-0.
(In press).
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Lewis, C;
Buchannan, J;
Clarke, A;
Clement, E;
Friedrich, B;
Hastings-Ward, J;
Hill, M;
... Lakhanpaul, M; + view all
(2021)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: awaiting peer review].
NIHR Open Research
, 1
, Article 23. 10.3310/nihropenres.13236.1.
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Lewis, C;
Simcock, IC;
Arthurs, OJ;
(2021)
Improving uptake of perinatal autopsy.
Current Opinion in Obstetrics and Gynecology
, 33
(2)
pp. 129-134.
10.1097/GCO.0000000000000691.
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Lewis, Celine;
Buchanan, James;
Clarke, Angus;
Clement, Emma;
Friedrich, Bettina;
Hastings-Ward, Jillian;
Hill, Melissa;
... Lakhanpaul, Monica; + view all
(2022)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol.
NIHR Open Research
, 1
, Article 23. 10.3310/nihropenres.13236.2.
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Lewis, C;
Hammond, J;
Hill, M;
Searle, B;
Hunter, A;
Patch, C;
Chitty, LS;
(2020)
Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100,000 genomes project.
European Journal of Medical Genetics
, 63
(11)
, Article 104043. 10.1016/j.ejmg.2020.104043.
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Lewis, C;
Hammond, J;
Klapwijk, JE;
Harding, E;
Lou, S;
Vogel, I;
Szepe, EJ;
... Riedijk, S; + view all
(2021)
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: an international cross-sectional study with healthcare professionals.
Prenatal Diagnosis
10.1002/pd.5932.
(In press).
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Lewis, C;
Hill, M;
Arthurs, OJ;
Hutchinson, C;
Chitty, LS;
Sebire, N;
(2018)
Factors Affecting Uptake of Postmortem Examination in the Prenatal, Perinatal and Paediatric Setting; a Systematic Review.
BJOG: An International Journal of Obstetrics and Gynaecology
, 125
(2)
pp. 172-181.
10.1111/1471-0528.14600.
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Lewis, C;
Hill, M;
Arthurs, OJ;
Hutchinson, JC;
Chitty, LS;
Sebire, N;
(2018)
Health professionals’ and coroners’ views on less invasive perinatal and paediatric autopsy: a qualitative study.
Archives of Disease in Childhood
, 103
(6)
pp. 572-578.
10.1136/archdischild-2017-314424.
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Lewis, C;
Hill, M;
Chitty, LS;
(2017)
Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
Prenatal Diagnosis
, 37
(11)
pp. 1130-1137.
10.1002/pd.5154.
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Lewis, C;
Hill, M;
Chitty, LS;
(2016)
A qualitative study looking at informed choice in the context of non-invasive prenatal testing for aneuploidy.
Prenatal Diagnosis
, 36
(9)
pp. 875-881.
10.1002/pd.4879.
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Lewis, C;
Hutchinson, JC;
Riddington, M;
Hill, M;
Arthurs, OJ;
Fisher, J;
Wade, A;
... Sebire, NJ; + view all
(2019)
Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study.
Health Technology Assessment
, 23
(46)
10.3310/hta23460.
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Lewis, C;
Latif, Z;
Hill, M;
Riddington, M;
Lakhanpaul, M;
Arthurs, OJ;
Hutchinson, JC;
... Sebire, NJ; + view all
(2018)
"We might get a lot more families who will agree": Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy.
PLoS One
, 13
(8)
, Article e0202023. 10.1371/journal.pone.0202023.
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Lewis, C;
Loe, BS;
Sidey-Gibbons, C;
Patch, C;
Chitty, LS;
Sanderson, SC;
(2019)
Development of a measure of genome sequencing knowledge for young people: The kids-KOGS.
Clinical Genetics
, 96
(5)
pp. 411-417.
10.1111/cge.13607.
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Lewis, C;
Riddington, M;
Hill, M;
Arthurs, OJ;
Hutchinson, JC;
Chitty, LS;
Bevan, C;
... Sebire, NJ; + view all
(2019)
Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed‐methods study with bereaved parents.
BJOG: An International Journal of Obstetrics & Gynaecology
, 126
(6)
pp. 745-753.
10.1111/1471-0528.15591.
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Lewis, C;
Riddington, M;
Hill, M;
Bevan, C;
Fisher, J;
Lyas, L;
Chalmers, A;
... Sebire, N; + view all
(2019)
"The communication and support from the health professional is incredibly important": A qualitative study exploring the processes and practices that support parental decision-making about postmortem examination.
Prenatal Diagnosis
, 39
(13)
pp. 1242-1253.
10.1002/pd.5575.
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Lewis, C;
Sanderson, S;
Hill, M;
Patch, C;
Searle, B;
Hunter, A;
Chitty, LS;
(2020)
Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study.
European Journal of Human Genetics
10.1038/s41431-020-0575-2.
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Lewis, C;
Sanderson, SC;
Hammond, J;
Hill, M;
Searle, B;
Hunter, A;
Patch, C;
(2020)
Development and mixed-methods evaluation of an online animation for young people about genome sequencing.
European Journal of Human Genetics
, 28
pp. 896-906.
10.1038/s41431-019-0564-5.
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Lou, S;
Lomborg, K;
Lewis, C;
Riedijk, S;
Petersen, OB;
Vogel, I;
(2020)
"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Acta Obstetricia et Gynecologica Scandinavica
, 99
(6)
pp. 791-801.
10.1111/aogs.13813.
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Mackley, Michael P;
Agrawal, Pankaj B;
Ali, Sara S;
Archibald, Alison D;
Dawson-McClaren, Belinda;
Ellard, Holly;
Freeman, Lucinda;
... McNeill, Alisdair; + view all
(2025)
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.
European Journal of Human Genetics
10.1038/s41431-025-01925-7.
(In press).
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Newlands, Fiona;
Lewis, Celine;
d'Oelsnitz, Anais;
Pinto Pereira, Snehal M;
Stephenson, Terence;
Chalder, Trudie;
Coughtrey, Anna;
... Shafran, Roz; + view all
(2024)
"People don't have the answers": A qualitative exploration of the experiences of young people with Long COVID.
Clinical Child Psychology and Psychiatry
10.1177/13591045241252463.
(In press).
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Oxenford, K;
Daley, R;
Lewis, C;
Hill, M;
Chitty, LS;
(2017)
Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study.
BMC Pregnancy and Childbirth
, 17
, Article 132. 10.1186/s12884-017-1315-7.
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Peter, Michelle;
Hammond, Jennifer;
Sanderson, Saskia C;
Gurasashvili, Jana;
Hunter, Amy;
Searle, Beverly;
Patch, Christine;
... Lewis, Celine; + view all
(2023)
Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project.
European Journal of Human Genetics
10.1038/s41431-023-01470-1.
(In press).
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Peter, Michelle;
Hammond, Jennifer;
Sanderson, Saskia C;
Gurasashvili, Jana;
Hunter, Amy;
Searle, Beverly;
Patch, Christine;
... Lewis, Celine; + view all
(2022)
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study.
European Journal of Human Genetics
10.1038/s41431-022-01065-2.
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Sanderson, SC;
Lewis, C;
Hill, M;
Peter, M;
McEntagart, M;
Gale, D;
Morris, H;
... Chitty, LS; + view all
(2021)
Decision-making, attitudes, and understanding among patients and relatives invited to undergo genome sequencing in the 100,000 Genomes Project: A multisite survey study.
Genetics in Medicine
10.1016/j.gim.2021.08.010.
(In press).
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Sanderson, SC;
Hill, M;
Patch, C;
Searle, B;
Lewis, C;
Chitty, LS;
(2019)
Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project.
BMJ Open
, 9
(11)
, Article e029699. 10.1136/bmjopen-2019-029699.
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Sanderson, SC;
Lewis, C;
Patch, C;
Hill, M;
Bitner-Glindzicz, M;
Chitty, LS;
(2018)
Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study.
Genetics in Medecine
, 21
pp. 1083-1091.
10.1038/s41436-018-0310-3.
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Sanderson, SC;
Loe, BS;
Freeman, M;
Gabriel, C;
Stevenson, DC;
Gibbons, C;
Chitty, L;
(2018)
Development of the Knowledge of Genome Sequencing (KOGS) questionnaire.
Patient Education and Counseling
, 101
(11)
pp. 1966-1972.
10.1016/j.pec.2018.07.011.
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Shelmerdine, SC;
Hutchinson, JC;
Lewis, C;
Simcock, IC;
Sekar, T;
Sebire, NJ;
Arthurs, OJ;
(2021)
A pragmatic evidence-based approach to post-mortem perinatal imaging.
Insights Imaging
, 12
(1)
, Article 101. 10.1186/s13244-021-01042-1.
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Siranosian, Jennifer;
Lewis, Celine;
Hill, Melissa;
Ormond, Kelly E;
(2023)
Exploring prenatal testing preferences among US pregnant individuals: A discrete choice experiment.
Journal of Genetic Counseling
10.1002/jgc4.1777.
(In press).
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Skirrow, H;
Foley, K;
Bedford, H;
Lewis, C;
Whittaker, E;
Costelloe, C;
Saxena, S;
(2023)
Impact of pregnancy vaccine uptake and socio-demographic determinants on subsequent childhood Measles, Mumps and Rubella vaccine uptake: A UK birth cohort study.
Vaccine
10.1016/j.vaccine.2023.11.063.
(In press).
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Xian Lim, Karen Mei;
Lewis, Celine;
Wong, Hung Chew;
Chong, Glenda Sze Ling;
Gosavi, Arundhati;
Choolani, Mahesh Arjandas;
(2022)
Does an educational video for aneuploidy screening improve informed choice among pregnant women? A randomised controlled trial.
Prenatal Diagnosis
10.1002/pd.6279.
(In press).
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